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Key considerations: How to build compliant software update practices for medical devices
Learn how to implement compliant software update practices for medical devices while navigating FDA and EU MDR regulations, ensuring safety and cybersecurity.
Mender Client 6.0 released
Discover the new features in Mender Client 6.0, including official Docker Compose support and enhanced network robustness for reliable IoT device updates.
Complying with the US FDA and EU MDR requires software updates
Ensuring compliance with US FDA and EU MDR for connected medical devices requires effective software updates, robust risk management, and thorough documentation throughout the product lifecycle.
IoT in 2026: Edge AI, growing complexity, and the demand for smarter updates
Explore the key trends shaping IoT in 2026, including Edge AI, hardware complexity, RTOS adoption, and the rise of AI-driven subscription models.
New Mender experimental AI-enabled feature
Discover Mender's new experimental AI feature that simplifies failure analysis for IoT device updates, saving time and effort for hosted Mender users.
Mender in 2025: A year in review with compliance, security, and AI-driven growth
A look at how regulatory compliance, security requirements, AI-driven scale, and OTA updates shaped device software management across the Mender ecosystem in 2025.
What’s new in Mender: Enhanced delta updates and user experience
Discover Mender's latest enhancements in delta updates and user experience, including server-side delta generation and user-friendly subscription management, in our newest product release.
Failed lifecycle management is unacceptable in FDA and MDR compliance
Ensure medical device compliance with FDA and EU MDR by adopting a lifecycle management strategy from design to post-market, focusing on continuous oversight and improvement.
The struggle to reach global markets for medical device manufacturers: The importance of international compliance
Navigating global regulatory compliance is crucial for medical device manufacturers. Learn strategies for documentation, software updates, and post-market surveillance to ensure international success and patient safety.